JP2000119242A - Hydrazine derivative composition and curable composition excellent in weatherability - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain the subject composition equipped with a low temperature- curing property and preservation stability simultaneously and capable of forming a membrane excellent in waterproof property, soil resistance, etc. by containing a specific polyhydrazine compound with a specific photostabilizer and/or an ultraviolet absorbing agent. SOLUTION: This hydrazine derivative composition contains (A) a polyhydrazine compound having >=2 hydrazine residues in one molecule, (B) a photostabilizer containing carbonyl group (preferably a hindered amine derivative) and/or an ultraviolet absorbing agent. The component A is preferably a semicarbazide derivative composition of the formula [R1 is a 2-20C alkylenediisocyanate, a 5-25C cycloalkylenediisocyanate or the like; R2 is H or a 1-20C alkyl; R3 is a 1-20C alkylene, a 5-20C cycloalkylene or the like; (n) is 0, 1; and (l), (m) are each 0 or a positive integer, provided that 20>=(l+m)>=3]. The composition is useful as a curing agent for a polycarbonyl compound, etc.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a hydrazine derivative composition and a curable composition having excellent weather resistance using the same. It is useful as an agent, a paper processing agent, or a finishing agent for woven or nonwoven fabrics. More specifically, the hydrazine derivative composition and the excellent hydrazine derivative composition which can be used in various applications as a clear coat agent, a top coat agent, a paint, an undercoat agent, a cloth or paper impregnating agent, an adhesive, etc. Curable composition.

[0002]

2. Description of the Related Art In recent years, aqueous emulsions have attracted attention in the field of coating as a conversion material from an organic solvent type to an aqueous type. However, they are still insufficient in water resistance, stain resistance, hardness, etc. as compared with organic solvent type coating agents. It does not show proper physical properties. For the purpose of improving these properties, it is common practice to introduce a functional group into an aqueous emulsion to form a crosslinked coating film.

As an aqueous emulsion for forming a crosslinked coating film, there is a great demand for a one-part, room-temperature curing type from the viewpoint of workability, workability, etc. In recent years, hydrazone crosslinking using a dehydration condensation reaction of a carbonyl group and a hydrazine group has been met. Aqueous emulsions have attracted attention. For example,
No. 20053, JP-A-57-3850, JP-A-57-3857, JP-A-58-96643, JP-A-4-249587, WO96 / 012
In pamphlet No. 52 and the like, by adding a polyfunctional carboxylic acid hydrazide compound or a semicarbazide derivative having a specific structure as a curing agent to a carbonyl group-containing aqueous emulsion, it has both low-temperature curability and storage stability,
A coating composition excellent in hardness, stain resistance and the like has been proposed.

[0004] However, the above coating composition forms a film excellent in stain resistance, hardness and the like, but sufficient performance has not yet been obtained in terms of weather resistance.

[0005]

An object of the present invention is to provide a film having both low-temperature curability and storage stability, and capable of forming a film excellent in water resistance, stain resistance, hardness and weather resistance.
An object of the present invention is to provide a hydrazine derivative composition and a curable composition using the same.

[0006]

Means for Solving the Problems The inventors have made intensive studies to solve the above-mentioned problems, and as a result, have reached the present invention. That is, a first aspect of the present invention is a hydrazine derivative composition comprising a polyhydrazine compound having two or more hydrazine residues in one molecule, a light stabilizer having a carbonyl group and / or an ultraviolet absorber having a carbonyl group. is there.

A second aspect of the invention is that the polyhydrazine compound is
The hydrazine derivative composition according to the first aspect, which is a semicarbazide derivative composition represented by the formula (1).

[0008]

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(Wherein R ¹ is a linear or branched alkylene diisocyanate having 2 to 20 carbon atoms, a cycloalkylene diisocyanate having 5 to 25 carbon atoms which may or may not have a substituent; Arylene diisocyanate having 6 to 20 carbon atoms which may or may not have a substituent,
And 8 to 20 carbon atoms which may or may not have a substituent
A polyisocyanate residue having no terminal isocyanate group, derived from at least one dimer to dimer oligomer of at least one diisocyanate selected from the group consisting of aralkylenediisocyanates, or R ¹ has ¹ carbon atom
Represents a triisocyanate residue having no terminal isocyanate group, which is derived from an alkylene diisocyanate having 2 to 20 carbon atoms which is substituted by an isocyanatoalkyl group having from 8 to 8 carbon atoms.

R ² independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; R ³ represents a linear or branched alkylene group having 1 to 20 carbon atoms;
Represents a cycloalkylene group having 0 or an arylene group having 6 to 10 carbon atoms which may or may not have a substituent.
n represents 0 or 1. l and m each represent 0 or a positive integer. However, 20 ≧ (l + m) ≧ 3. A third aspect of the present invention is the hydrazine derivative composition according to the first or second aspect, wherein the light stabilizer having a carbonyl group is a hindered amine derivative.

A fourth aspect of the present invention is a curable composition containing the hydrazine derivative composition according to any one of the first to third aspects of the present invention and a polycarbonyl compound and / or a polyepoxy compound. A fifth aspect of the present invention is the curable composition according to the fourth aspect of the present invention, which contains a monoketone represented by the formula (2).

R ⁴ R ⁵ C ＝ O (2) (wherein R ⁴ and R ⁵ are each a hydrogen atom, a linear or branched aliphatic residue having 2 to 20 carbon atoms,
Represents an alicyclic residue having 20 carbon atoms, or an aromatic residue which may or may not have a substituent. R ⁴ and R ⁵ may form a cyclic structure. A sixth aspect of the present invention is the curable composition according to the fourth or fifth aspect, wherein the polycarbonyl compound is an aqueous dispersion of an acrylic copolymer containing a carbonyl group.

A seventh aspect of the present invention is the curable composition according to the fourth or fifth aspect, wherein the polyepoxy compound is an aqueous dispersion of an acrylic copolymer containing an epoxy group. Hereinafter, the present invention will be described in detail. In the present invention, one hydrazine residue is used.
A polyhydrazine compound having two or more in a molecule is defined as 1
A compound having two or more hydrazine residues represented by the formula (3) in the molecule.

-NR ² NH ₂ (3) (wherein R ² represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms.) A monohydrazine compound having only one hydrazine residue in one molecule is It is not preferable because it has no or very low cross-linking ability with respect to a polycarbonyl compound described later.

Examples of the polyhydrazine compound include polyhydrazide compounds, polysemicarbazide compounds, and carbonated polyhydrazides represented by the formula (4).

[0016]

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(Wherein x represents an integer of 0 to 20) Specific examples of the polyhydrazide compound include oxalic acid dihydrazide, malonic acid dihydrazide, succinic acid dihydrazide,
Glutaric acid dihydrazide, adipic acid dihydrazide, pimelic acid dihydrazide, suberic acid dihydrazide, azelaic acid dihydrazide, sebacic acid dihydrazide, dodecanediohydrazide, hexadecandiohydrazide,
1,4-cyclohexanedihydrazide, tartaric acid dihydrazide, malic acid dihydrazide, iminodiacetic acid dihydrazide, maleic acid dihydrazide, fumaric acid dihydrazide,
Itaconic dihydrazide, isophthalic dihydrazide,
Terephthalic dihydrazide, 2,6-naphthoic dihydrazide, 1,4-naphthoic dihydrazide, 4,4'-
Dicarboxylic acid dihydrazides such as bisbenzene dihydrazide and 2,6-pyridine dihydrazide; tricarboxylic acid trihydrazides such as 1,3,5-cyclohexanetricarboxylic acid trihydrazide, trimellitic acid trihydrazide, citric acid trihydrazide and nitriloacetic acid trihydrazide. , Pyromellitic acid tetrahydrazide, 1,4,5
Examples thereof include tetracarboxylic acid tetrahydrazides such as 8-naphthoic acid tetrahydrazide and ethylenediaminetetraacetic acid tetrahydrazide, and acid hydrazide polymers represented by the formula (5) and having a number average molecular weight of 500 to 500,000 or a combination thereof. Can be

[0018]

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Wherein X is a hydrogen atom or a carboxyl group, Y is a hydrogen atom or a methyl group, and A is a monomer selected from acrylamide, methacrylamide, acrylate, methacrylate and maleic anhydride. And B is a polymerized unit of a monomer copolymerizable with acrylamide, methacrylamide, acrylate, methacrylate, and maleic anhydride, and l, m and n are as follows: The following shows the mole fraction of each component that satisfies each of the equations.

2 mol% ≦ l ≦ 100 mol% 0 mol% ≦ m + n ≦ 98 mol% l + m + n = 100 mol% The acid hydrazide-based polymer may be a random copolymer or a block copolymer. Of the polyhydrazine compounds according to the present invention, polysemicarbazide compounds are most preferred because of their good hydrolysis resistance of hydrazine residues.

Specific examples of the polysemicarbazide compound include a semicarbazide derivative represented by the formula (1) and a bissemicarbazide represented by the formula (6).

[0022]

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Wherein R ¹ is a linear or branched alkylene diisocyanate having 2 to 20 carbon atoms, a cycloalkylene diisocyanate having 5 to 25 carbon atoms which may or may not have a substituent; Arylene diisocyanate having 6 to 20 carbon atoms which may or may not have a substituent,
And 8 to 20 carbon atoms which may or may not have a substituent
A polyisocyanate residue having no terminal isocyanate group, derived from at least one dimer to dimer oligomer of at least one diisocyanate selected from the group consisting of aralkylenediisocyanates, or R ¹ has ¹ carbon atom
Represents a triisocyanate residue having no terminal isocyanate group, which is derived from an alkylene diisocyanate having 2 to 20 carbon atoms which is substituted by an isocyanatoalkyl group having from 8 to 8 carbon atoms.

R ² each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. R ³ is a linear or branched alkylene group having 1 to 20 carbon atoms,
Represents a cycloalkylene group having 20 or an arylene group having 6 to 10 carbon atoms which may or may not have a substituent.

N represents 0 or 1. l and m each represent 0 or a positive integer. However, 20 ≧ (l + m) ≧ 3
It is. )

[0026]

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(Wherein, R ⁶ is a linear or branched divalent aliphatic residue having 2 to 20 carbon atoms;
Divalent alicyclic residue, divalent aromatic residue having 6 to 25 carbon atoms which may or may not have a substituent, and carbon which may or may not have a substituent It represents a divalent aromatic alicyclic residue of the formulas 6 to 25. R ² each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. When the semicarbazide derivative represented by the formula (1) among the above polysemicarbazide compounds is used as a curing agent for a curable composition, it is polyfunctional and has compatibility with a polycarbonyl compound and the like described later. Since it is good, a cross-linking ability is high, and a tough film having excellent water resistance can be obtained.

The semicarbazide derivative represented by the formula (1) can be obtained by reacting a polyisocyanate compound having three or more —NCO groups in one molecule with a hydrazine derivative. Examples of the polyisocyanate compound having three or more -NCO groups in one molecule include oligomerization by forming a diisocyanate compound into a buret bond, a urea bond, an isocyanurate bond, a urethane bond, an allophanate bond, a uretdione bond, or the like. Polyisocyanate compounds, and combinations thereof.

Examples of the above diisocyanate compounds include alkylene diisocyanates such as hexamethylene diisocyanate (HDI), 4,4'-methylenebiscyclohexyl diisocyanate (hydrogenated MDI), isophorone diisocyanate (IPDI), and dimethylcyclohexane diisocyanate (hydrogenated). XDI), 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate and a mixture thereof (TDI), diphenylmethane-4,4'-diisocyanate (MDI), naphthalene-1,5-diisocyanate ( NDI), 3,3-dimethyl-4,4-
Biphenylene diisocyanate (TODI), crude TD
I, polymethylene polyphenyl diisocyanate, crude MDI, arylene diisocyanate such as phenylene diisocyanate, xylylene diisocyanate (XD
Aralkylenediisocyanates such as I) and the like, and combinations thereof.

Of these diisocyanate compounds, alkylene diisocyanate and cycloalkylene diisocyanate are preferred from the viewpoint of improving heat resistance yellowing, weather resistance and the like of a film using the composition containing the resulting semicarbazide derivative. Furthermore, in addition to the above-mentioned polyisocyanate compounds, alkylene diisocyanates having 2 to 20 carbon atoms and substituted with an isocyanatoalkyl group having 1 to 8 carbon atoms, such as 1,8-diisocyanato-4-isocyanatomethyloctane, etc. From the viewpoint of compatibility with a polycarbonyl compound described below, it is preferable to use the above-described polyisocyanate compound obtained by oligomerizing a diisocyanate compound.

In the present invention, the semicarbazide derivative synthesized using the polyisocyanate compound having three or more —NCO groups in one molecule is polyfunctional, and can provide a high crosslink density and a tough film. If the number of semicarbazide groups in one molecule is too large, the viscosity of the generated semicarbazide derivative becomes high and handling becomes difficult. Therefore, the number of -NCO groups in one molecule of the polyisocyanate compound used for the synthesis of the semicarbazide derivative is preferably 3 to 20.

Of these polyisocyanate compounds, the semicarbazide derivative derived therefrom has excellent compatibility with the polycarbonyl compound and the like described below, and the hardness of the film formed from the curable composition containing the semicarbazide derivative Preferred examples from the viewpoint of chemical resistance, heat resistance, and the like include those having an isocyanurate structure or a burette structure as a basic skeleton. Further, as a film having excellent flexibility of a film obtained from a curable composition with a polycarbonyl compound or the like, for example, a film having a urethane structure as a basic skeleton may be mentioned.

Examples of the polyisocyanate compound having an isocyanurate structure as a basic skeleton include an isocyanurate-type polyisocyanate of hexamethylene diisocyanate described in JP-A-55-38380 and JP-A-57-78460. Copolymerized isocyanurate-type polyisocyanate of isophorone diisocyanate and hexamethylene diisocyanate as described in JP-A-57-47321, and isocyanurate modified with a polyfunctional alcohol as described in JP-A-57-47321. Low-viscosity isocyanurate-type polyisocyanate as described in JP-A-64-33115.
A cyclic trimerization reaction of a diisocyanate compound in the presence of a catalyst, such as a highly branched isocyanurate-type polyisocyanate described in US Pat. %, Preferably 10 to 60% by weight, and a polyisocyanate compound having an isocyanurate structure obtained by removing and purifying an excess diisocyanate compound.

Examples of the polyisocyanate compound having a bullet structure as a basic skeleton include, for example, those described in
No. 106797, JP-A-55-11452 and the like, hexamethylene diisocyanate-based bullet type polyisocyanate,
No. 95259, a copolymer of isophorone diisocyanate and hexamethylene diisocyanate represented by a burette-type polyisocyanate and the like. Agent / diisocyanate in an equivalent ratio of 1/2 to 1/100, preferably 1
After reacting at / 3 to 1/50, a polyisocyanate compound having a buret structure obtained by removing and purifying an excess diisocyanate compound is exemplified.

Examples of polyisocyanate compounds having a urethane structure as a basic skeleton include, for example, JP-A-61-2
No. 8518 and JP-A-4-50277, etc., after reacting polycaprolactone polyol and diisocyanate at an equivalent ratio of -NCO / -OH of 5 to 40, and removing and purifying excess diisocyanate. The resulting urethane-type polyisocyanate is exemplified. In particular, when the molecular weight is less than 2,000, in addition to flexibility, water resistance, heat resistance and the like are excellent, and high hardness can be exhibited.

Examples of the hydrazine derivative to be reacted with the polyisocyanate compound include hydrazine and hydrates thereof, monoalkylhydrazines such as methylhydrazine and ethylhydrazine, ethylene-1,2-dihydrazine, and the like.
Propylene-1,3-dihydrazine, butylene-1,4
Dihydrazine compounds such as dihydrazine, oxalic acid dihydrazide, malonic acid dihydrazide, succinic dihydrazide,
Dicarboxylic acid dihydrazides such as glutaric acid dihydrazide, adipic acid dihydrazide, sebacic acid dihydrazide, maleic acid dihydrazide, fumaric acid dihydrazide, itaconic acid dihydrazide, isophthalic acid dihydrazide, phthalic acid dihydrazide, etc .; Examples include carbonic acid polyhydrazides represented by the following general formula (4), bissemicarbazides represented by the following general formula (6), and the like, and combinations thereof.

[0037]

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(Where x represents an integer of 0 to 20)

[0039]

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(Wherein R ⁶ is a linear or branched divalent aliphatic residue having 2 to 20 carbon atoms;
Divalent alicyclic residue, divalent aromatic residue having 6 to 25 carbon atoms which may or may not have a substituent, and carbon which may or may not have a substituent It represents a divalent aromatic alicyclic residue of the formulas 6 to 25. R ² each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. In the production of the above semicarbazide derivative, the equivalent ratio of the NCO group of the above-mentioned polyisocyanate compound to the —NR ² NH ₂ group or the group that can be converted to —NR ² NH ₂ group in the hydrazine derivative is 1: 1. The ratio is from 2 to 100, preferably from 1: 2 to 80, and more preferably from 1: 4 to 50. When the equivalent ratio is less than 1: 1.2, the product has a high molecular weight and the increase in viscosity is not preferable. If the ratio is more than 1: 100, unreacted hydrazine derivatives are undesirably present in large amounts. (Here, R ² of the —NR ² NH ₂ group represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms.) After producing the semicarbazide derivative, excess hydrazine derivative may be removed by distillation, extraction, or the like as necessary. Can be.

The semicarbazide derivative can be produced without a solvent or in a solvent. Solvents that are inert to the NCO groups or that are less active than the reaction components can be used. The solvent may remain in the semicarbazide derivative, but can also be removed by distillation by heating under normal pressure or reduced pressure. In the present invention, a hydrazine derivative composition comprising the above polyhydrazine compound and a light stabilizer having a carbonyl group capable of reacting with the polyhydrazine compound and / or an ultraviolet absorber having a carbonyl group capable of reacting with the polyhydrazine compound Hydrazine derivative composition capable of forming a film having both low-temperature curability and storage stability, and having excellent water resistance, stain resistance, hardness and weather resistance, and a curable composition using them Can be provided.

Examples of the light stabilizer having a carbonyl group in the present invention include a hindered phenol derivative having a carbonyl group and a hindered amine derivative having a carbonyl group. In addition, examples of the ultraviolet absorber having a carbonyl group in the present invention include a benzophenone derivative having a carbonyl group, a benzotriazole derivative having a carbonyl group, and a triazine derivative having a carbonyl group.

Among these light stabilizers having a carbonyl group and ultraviolet absorbers having a carbonyl group, hindered amine derivatives having a carbonyl group, especially 2,2,6,
6-Tetraalkyl-piperidine derivatives are preferred. Examples of the 2,2,6,6-tetraalkyl-piperidine derivative having a carbonyl group include 2,2,6,6-tetraalkyl-piperidones represented by the formula (7).

[0044]

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In the formula, R ⁷ represents a hydrogen atom, an oxy group, a hydroxy group, a halogen atom, a linear or branched alkyl group having 1 to 30 carbon atoms which may or may not have a substituent. 5 to 2 carbon atoms which may or may not have a group or a substituent
A cycloalkyl group of 0, a benzyl group having 7 to 30 carbon atoms which may or may not have a substituent, a phenyl group having 6 to 30 carbon atoms which may or may not have a substituent, An acyl group having 2 to 30 carbon atoms which may or may not have a substituent,
An alkoxy group having 1 to 30 carbon atoms which may or may not have a substituent, an alkoxycarbonyl group having 1 to 30 carbon atoms which may or may not have a substituent, or the following formula (8 )
Represents a group represented by

-(CH_TwoCHR^TenO-)_sR¹¹ (8) (where R^TenIs a linear group which may or may not have a substituent
Represents a branched or branched alkyl group having 1 to 30 carbon atoms.
R¹¹May or may not have a hydrogen atom and a substituent
A linear or branched alkyl group having 1 to 30 carbon atoms,
C 5-20 carbons which may or may not have a substituent
Roalkyl groups, carbons with or without substituents
7 to 30 benzyl groups, even if they have a substituent
Represents a phenyl group having 6 to 30 carbon atoms. Also, s is
Represents an integer of 2 to 80. ) R⁸, R ⁹Are the same but different
A hydrogen atom or an alkyl group having 1 to 10 carbon atoms
Representsの Of the 2,2,6,6-tetraalkyl-piperidone
As a specific example, 2,2,6,6-tetramethyl-4-
Piperidone, N-methyl-2,2,6,6-tetramethi
4-piperidone, N-ethyl-2,2,6,6-te
Tramethyl-4-piperidone, N-benzyl-2,2,
6,6-tetramethyl-4-piperidone, N-bromo-
2,2,6,6-tetramethyl-4-piperidone, N-
Oxy-2,2,6,6-tetramethyl-4-piperide
, N-nitroso-2,2,6,6-tetramethyl-4
-Piperidone, N-allyl-2,2,6,6-tetrame
Tyl-4-piperidone, N-dodecyl-2,2,6,6
-Tetramethyl-4-piperidone, N-ethoxycarbo
Nyl-2,2,6,6-tetramethyl-4-piperide
, N-acetyl-2,2,6,6-tetramethyl-4
-Piperidone, N-beta-cyanoethyl-2,2,
6,6-tetramethyl-4-piperidone, N-beta
Hydroxyethyl-2,2,6,6-tetramethyl-
4-piperidone, N-methoxy-2,2,6,6-tet
Lamethyl-4-piperidone, N-methoxypoly (ethoxy
B) Ethyl-2,2,6,6-tetramethyl-4-pipe
Lidone, N-nonylphenoxypoly (ethoxy) ethyl
-2,2,6,6-tetramethyl-4-piperidone,
2,2,6,6-tetraethyl-3,5-dimethyl-4
-Piperidone, 2,3,6-trimethyl-2,6-die
Tyl-4-piperidone and the like.

In the hydrazine derivative composition of the present invention, the polyhydrazine compound and the light stabilizer having a carbonyl group and / or the ultraviolet absorber having a carbonyl group can be mixed at any ratio. Ratio of the carbonyl group in the light stabilizer having a carbonyl group to the hydrazine residue and / or the ultraviolet absorber having the carbonyl group is (carbonyl group) /
The molar ratio of (hydrazine residue) is preferably in the range of 0.001 to 10.

The mixing of the polyhydrazine compound and the light stabilizer having a carbonyl group and / or the ultraviolet absorber having a carbonyl group can be carried out in an arbitrary temperature range without a solvent or in a solvent. Specific examples of the solvent include water, t-butanol, isopropanol,
Alcohols such as 2-butoxyethanol; ether solvents such as dioxane, tetrahydrofuran and diethylene glycol dimethyl ether; amide solvents such as dimethylformamide and dimethylacetamide; lactam solvents such as N-methyl-2-pyrrolidone; and sulfoxides such as dimethyl sulfoxide. Examples thereof include system solvents, ester solvents such as ethyl acetate and cellosolve acetate, aromatic hydrocarbon solvents such as toluene and xylene, aliphatic hydrocarbon solvents such as n-hexane, and the like, and combinations thereof.

The hydrazine derivative composition of the present invention contains a hydrophilic group-containing compound represented by the formula (9) described in JP-A-8-245878 and a ketone for the purpose of assisting dispersion stability and solubility in an aqueous medium. An acid and / or a salt thereof or a surfactant may be used in combination.

[0050]

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(Wherein, R ¹² represents a residue obtained by removing an NCO group from a polyisocyanate compound. P and q each represent 0 or a positive integer, r represents a positive integer.
+ P + q) ≧ 2. A represents an organic group having a nonionic hydrophilic group and / or an ionic (including those which can be converted into an ionic) hydrophilic group. R ³ may have a divalent linear or branched aliphatic residue having 2 to 20 carbon atoms or an alicyclic residue having 5 to 20 carbon atoms or a substituent. Represents an aromatic residue which may not be present. n represents 0 or 1. Examples of the ketone acid include pyruvic acid, levulinic acid, acetoacetic acid, propionylacetic acid, benzoylformic acid,
Monoketone carboxylic acids such as phenylpyruvic acid, ketocapric acid, ketoundecanoic acid, ketostearic acid, ketoheneicosenoic acid, benzoylacetic acid, benzoylpropionic acid, and ketoglyconic acid, ketomalonic acid, acetonedicarboxylic acid, 2-ketoglutaric acid, acetonediene Examples thereof include monoketone dicarboxylic acids such as acetic acid and acetone dipropionic acid and the like, and combinations thereof.

The ketone acid salt can be obtained by neutralizing the ketone acid with a base. Examples of the base used for neutralization include hydroxides of alkali metals such as KOH, NaOH, and LiOH, amines, and the like, and combinations thereof. Examples of the surfactant include higher fatty acids, resin acids, acidic fatty alcohols, sulfates, higher alkylsulfonic acids, alkylallyl sulfonates,
Anionic surfactants represented by salts such as sulfonated castor oil, sulfosuccinates, and alkenyl succinic acids; and known reaction products of ethylene oxide with long-chain fatty alcohols or phenols and phosphoric acids Examples thereof include a nonionic surfactant, a cationic surfactant containing a quaternary ammonium salt or the like, a polymer dispersion stabilizer such as (partially saponified) polyvinyl alcohol, and the like, and a combination thereof.

The hydrazine derivative composition obtained in the present invention has reactivity to a polycarbonyl compound or a polyepoxy compound, light stability and / or ultraviolet absorption, and therefore has a water resistance and a water absorption which cannot be attained conventionally. In addition to various curing performances, excellent weather resistance can be exhibited. Therefore, the hydrazine derivative composition of the present invention is useful as a (particularly aqueous) curing agent for a polycarbonyl compound and / or a polyepoxy compound. The fourth curable composition of the present invention is the hydrazine derivative composition described above. And a polycarbonyl compound and / or a polyepoxy compound. Among the curable compositions, the combination of the aqueous hydrazine derivative composition and the polycarbonyl compound has excellent storage stability, and provides a film excellent in weather resistance, water resistance, stain resistance, hardness and the like. It is particularly preferable because it can be given at a low temperature.

As the polycarbonyl compound, for example, a copolymer containing a carbonyl group, JP-A-2-2380
No. 15, carbonyl group-containing polyurethanes starting from a mono- or polyalcohol having a carbonyl group such as hydroxyacetone, acetoacetylated polyvinyl alcohol, and JP-A-9-32409.
As described in JP-A No. 5 (1994), polyvinyl alcohol-based resins having a diacetone group in a side chain, acetoacetylated hydroxyalkylcellulose, and the like, and a combination thereof can be used.

Among these, preferred polycarbonyl compounds are carbonyl group-containing ethylenically unsaturated monomers (a)
And a carbonyl group-containing copolymer obtained by copolymerizing the monomer (A) with an ethylenically unsaturated monomer (B) copolymerizable with the monomer (A), and more preferably a polycarbonyl compound. Is 0.1 to 30% by weight of a carbonyl group-containing ethylenically unsaturated monomer (a) and an ethylenically unsaturated monomer (b) 7 copolymerizable with the monomer (a).
A carbonyl group-containing copolymer obtained by copolymerizing 0 to 99.9% by weight.

Examples of the carbonyl group-containing ethylenically unsaturated monomer (a) include diacetone acrylamide, diacetone methacrylamide, acrolein, vinyl methyl ketone, acetoacetoxyethyl methacrylate, acetoacetoxyethyl acrylate, formylstyrene, and the like. Combination is mentioned. Examples of the ethylenically unsaturated monomer (b) copolymerizable with the monomer (a) include acrylic acid esters, methacrylic acid esters, ethylenically unsaturated monomers having a carboxyl group, and ethylene having an epoxy group. Unsaturated monomers, acrylamide-based monomers, methacrylamide-based monomers, vinyl cyanides, and the like. Examples of (meth) acrylates include those having 1 to 18 carbon atoms in the alkyl portion. (Meth) acrylic acid alkyl ester, (meth) acrylic acid hydroxyalkyl ester having 1 to 18 carbon atoms in the alkyl part, 1 to 100 (poly) oxyethylene (meth) acrylate having 1 to 100 ethylene oxide groups, propylene (Poly) oxypropylene (meth) acrylate having 1 to 100 oxide groups and 1 to 100 ethylene oxide groups Poly) oxyethylene di (meth) acrylate. Specific examples of the (meth) acrylate include methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, methyl (meth) acrylate Cyclohexyl, dodecyl (meth) acrylate and the like. Specific examples of the hydroxyalkyl (meth) acrylate include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate,
2-hydroxycyclohexyl (meth) acrylate,
Dodecyl (meth) acrylate and the like. (Poly)
Specific examples of oxyethylene (meth) acrylate include ethylene glycol (meth) acrylate, ethylene glycol methoxy (meth) acrylate, diethylene glycol (meth) acrylate, diethylene glycol methoxy (meth) acrylate, and tetramethyl (meth) acrylate. Examples include ethylene glycol and tetraethylene glycol methoxy (meth) acrylate. Specific examples of (poly) oxypropylene (meth) acrylate include:
Propylene glycol (meth) acrylate, propylene glycol methoxy (meth) acrylate, dipropylene glycol (meth) acrylate, dipropylene glycol methoxy (meth) acrylate, tetrapropylene glycol (meth) acrylate, methoxy (meth) acrylic Acid tetrapropylene glycol and the like. Specific examples of (poly) oxyethylene di (meth) acrylate include ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, diethylene glycol methoxy (meth) acrylate, and di (meth) acrylate.
Examples include tetraethylene glycol acrylate.

Specific examples of the ethylenically unsaturated monomers having a carboxyl group include acrylic acid, methacrylic acid,
There are itaconic acid, fumaric acid, maleic acid, maleic acid half ester, crotonic acid and the like. Examples of (meth) acrylamide monomers include (meth) acrylamide, N-methylol (meth) acrylamide, N-butoxy Examples include methyl (meth) acrylamide, and examples of vinyl cyanides include (meth) acrylonitrile.

Specific examples of the ethylenically unsaturated monomers having an epoxy group include glycidyl (meth) acrylate,
(Meth) acrylic acid 2,3-cyclohexene oxide, allyl glycidyl ether and the like can be mentioned. Specific examples other than the above include, for example, olefins such as ethylene, propylene and isobutylene, dienes such as butadiene, haloolefins such as vinyl chloride and vinylidene chloride, vinyl acetate, vinyl propionate, n-vinyl butyrate, and benzoic acid. Vinyl acid, vinyl pt-butyl benzoate,
Vinyl carboxylate esters such as vinyl pivalate, vinyl 2-ethylhexanoate, vinyl versatate and vinyl laurate; carboxylate isopropenyl esters such as isopropenyl acetate and isopropenyl propionate; ethyl vinyl ether, isobutyl vinyl ether and cyclohexyl Vinyl ethers such as vinyl ether; aromatic vinyl compounds such as styrene and vinyl toluene; allyl esters such as allyl acetate and allyl benzoate; allyl ethers such as allyl ethyl ether and allyl phenyl ether; and γ- (meth) acryloxy Propyltrimethoxysilane, 4- (meth) acryloyloxy-2,2,6,6-tetramethylpiperidine, 4- (meth) acryloyloxy-1,2,2,
6,6, -pentamethylpiperidine, perfluoromethyl (meth) acrylate, perfluoropropyl (meth) acrylate, perfluoropropyromethyl (meth) acrylate, vinylpyrrolidone, trimethylolpropane tri (meth) acrylate, (meth) Examples include allyl acrylate and the like, and combinations thereof.

The polycarbonyl compound is preferably obtained by suspension polymerization, emulsion polymerization or solution polymerization, and more preferably an aqueous dispersion (emulsion) obtained by emulsion polymerization. Further, a carbonyl group-containing acrylic copolymer aqueous dispersion using an acrylic monomer is preferable.

The polycarbonyl compound is an anionic ethylene selected from the group consisting of ethylenically unsaturated monomers having a sulfonic acid group or a sulfonate group, ethylenically unsaturated monomers having a sulfate group, and mixtures thereof. It is preferably obtained by copolymerization in the presence of the unsaturated monomer (c). The ethylenically unsaturated monomer having a sulfonic acid group or a sulfonate group has a radically polymerizable double bond, and is partially substituted with a group that is an ammonium salt, a sodium salt, or a potassium salt of a sulfonic acid group. And an alkyl group having 1 to 20 carbon atoms, an alkyl ether group having 2 to 4 carbon atoms, a polyalkyl ether group having 2 to 4 carbon atoms, an aryl group having 6 or 10 carbon atoms, and a succinic acid group. The compound is a compound having a substituent or a vinylsulfonate compound having a vinyl group to which an ammonium salt, a sodium salt or a potassium salt of a sulfonic acid group is bonded.

The ethylenically unsaturated monomer having a sulfate group has a radically polymerizable double bond and is partially substituted by a group which is an ammonium, sodium or potassium salt of the sulfate group. Has 1-2 carbon atoms
0 alkyl group, alkyl ether group having 2 to 4 carbon atoms,
It is a compound having a substituent selected from the group consisting of a polyalkyl ether group having 2 to 4 carbon atoms and an aryl group having 6 or 10 carbon atoms.

As specific examples of the compound having a succinic acid group partially substituted by a group which is an ammonium salt, a sodium salt or a potassium salt of a sulfonic acid group, allyl sulfosuccinates such as those represented by formulas (10) and (11) ), (1)
2) and (13).

[0063]

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[0064]

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[0065]

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[0066]

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In the formulas (10) to (13), R ^{1 ′} is hydrogen or a methyl group, and R ^{2 ′} is a cycloalkyl group having 5 to 12 carbon atoms, an aryl group having 5 to 10 carbon atoms, 6-1
9 or a hydrocarbon group such as an aralkyl group or a part of which is substituted with a hydroxyl group, a carboxylic acid group or the like, or a polyoxyalkylene alkyl ether group (the alkyl portion has 0 to 20 carbon atoms and the alkylene portion has Is 2-4),
An organic group containing an alkylene oxide compound such as a polyoxyalkylene alkylphenyl ether group (the alkyl portion has 0 to 20 carbon atoms and the alkylene portion has 2 to 4 carbon atoms). A is an alkylene group having 2 to 4 carbon atoms or a substituted alkylene group. n is an integer of 0 to 200. M is ammonium, sodium, or potassium.と し て As a compound containing the above formulas (10) and (11), for example, Eleminor JS-2 (trade name) (Sanyo Chemical Co., Ltd.)
And those containing the above formulas (12) and (13) include, for example, Latemul S-120, S-180A or S-180 (trade name) (manufactured by Kao Corporation).

An alkyl ether group having 2 to 4 carbon atoms or a C 2 to C 4 partially substituted by a group which is an ammonium salt, a sodium salt or a potassium salt of a sulfonic acid group.
Examples of the compound having a polyalkyl ether group of 4 include a compound represented by the formula (14) or (15).

[0069]

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(Wherein each of R ^{3 ′} and R ^{4 ′} is independently an alkyl group, alkenyl group or aralkyl group having 6 to 18 carbon atoms, and R ^{5 ′} is hydrogen or propenyl group). A is an alkylene group having 2 to 4 carbon atoms, and n is 1
It is an integer of ~ 200. M is ammonium, sodium or potassium. )

[0071]

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Wherein R ^{6 ′} is hydrogen or a methyl group, R ^{7 ′} is an alkyl group or an acyl group having 8 to 24 carbon atoms, and A is an alkylene group having 2 to 4 carbon atoms. Is an integer of 0 to 20, n is an integer of 0 to 50. M
Is ammonium, sodium or potassium. As the alkylphenol ether-based compound represented by the above formula (14), there is, for example, Aqualon HS-10 (trade name) (manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), and the above formula (15)
As a compound represented by, for example, Adecaria Soap SE
-1025N (trade name) (manufactured by Asahi Denka Kogyo KK).

Other specific examples of the compound having an aryl group partially substituted by a sulfonate group include p-
Ammonium, sodium and potassium salts of styrene sulfonic acid. Examples of the vinyl sulfonate compound having a vinyl group to which a group which is an ammonium salt, a sodium salt or a potassium salt of a sulfonic acid group is bonded include, for example, alkylsulfonic acid (meth) acrylate such as 2-sulfoethylacrylate and methylpropanesulfonic acid ( And ammonium salts such as (meth) acrylamide and allylsulfonic acid, sodium salts and potassium salts.

Examples of the compound having an alkyl ether group having 2 to 4 carbon atoms or a polyalkyl ether group having 2 to 4 carbon atoms, which is partially substituted by an ammonium salt, a sodium salt or a potassium salt of a sulfate ester group, include: And a compound having an alkyl ether group partially substituted with a sulfonate group, represented by the formulas (14) and (15).

These anionic ethylenically unsaturated monomers (c) exist in the emulsion as a copolymer obtained by radical polymerization of the emulsion particles, or are adsorbed as unreacted substances to the emulsion particles, or the emulsion aqueous phase It is present in the emulsion particles, or is adsorbed to emulsion particles as a copolymer with a water-soluble monomer or a copolymer of monomers, or is present in an emulsion aqueous phase.

By increasing the ratio of the particular states, the water resistance of the film obtained from the emulsion can be improved. Further, the anionic ethylenically unsaturated monomer (c) is obtained by pyrolysis gas chromatogram mass spectrometry (Py-GC) of a film obtained from the emulsion.
-MS) or pyrolysis mass spectrometry (Py-MS). Another method is to separate the aqueous phase component of the emulsion and then use fast atom bombardment mass spectrometry (FAB).
Mass spectrum).

In the production of the emulsion, a normal surfactant can be used in addition to the anionic ethylenically unsaturated monomer (c). For example, anionic surfactants such as fatty acid soaps, alkyl sulfonates, alkyl sulfosuccinates, polyoxyethylene alkyl sulfates, polyoxyethylene alkyl aryl sulfates, polyoxyethylene alkyl aryl ethers, and polyoxyethylene sorbitan fatty acid esters , Non-reactive nonionic surfactants such as oxyethyleneoxypropylene block copolymers, α- [1-[(allyloxy) methyl] -2-
(Nonylphenoxy) ethyl] -ω-hydroxypolyoxyethylene (trade name: Adecaria Soap NE-20,
NE-30, NE-40, etc., manufactured by Asahi Denka Kogyo Co., Ltd.), polyoxyethylene alkylpropenyl phenyl ether (trade names: Aqualon RN-10, RN-20, RN-
Nonionic surfactants copolymerized with an ethylenically unsaturated monomer referred to as a reactive nonionic surfactant, such as No. 30, RN-50, etc., manufactured by Daiichi Pharmaceutical Co., Ltd.).

In obtaining the polycarbonyl compound,
Radical polymerization catalysts are those that undergo radical decomposition by heat or a reducing substance to cause addition polymerization of ethylenically unsaturated monomers, and include water-soluble or oil-soluble persulfates, peroxides, azobis compounds, and the like. used. Examples thereof include potassium persulfate, sodium persulfate, ammonium persulfate, hydrogen peroxide, t-butyl hydroperoxide, t-butyl peroxybenzoate, 2,2
-Azobisisobutyronitrile, 2,2-azobis (2
-Diaminopropane) hydrochloride, 2,2-azobis (2,4-dimethylvaleronitrile) and the like,
The amount is usually 0.1 to 1% by weight based on the ethylenically unsaturated monomer. Usually under normal pressure, 65-9
It is preferable to carry out the polymerization at a polymerization temperature of 0 ° C., but it is also possible to carry out the polymerization under a high pressure in accordance with the characteristics such as the vapor pressure at the polymerization temperature of the monomer. When acceleration of the polymerization rate and low-temperature polymerization at 70 ° C. or lower are desired, for example, sodium bisulfite, ferrous chloride, ascorbate,
It is advantageous to use a reducing agent such as Rongalite in combination with a radical polymerization catalyst. In order to further control the molecular weight, a chain transfer agent such as dodecyl mercaptan can be optionally added.

In the fourth aspect of the present invention, in order to keep the polycarbonyl compound stable for a long period of time, it is preferable to adjust the pH to the range of 5 to 10, and if necessary, ammonia, sodium hydroxide, potassium hydroxide, dimethylaminoethanol And the like, and acids such as hydrochloric acid, sulfuric acid, acetic acid, lactic acid and the like can also be added. Examples of the polyepoxy compound that can be used in the fourth curable composition of the present invention include an epoxy group-containing ethylenically unsaturated monomer such as glycidyl (meth) acrylate as an essential component and other unsaturated compounds. Monomer and bulk polymerization, suspension polymerization, emulsion polymerization,
A copolymer containing an epoxy group obtained by copolymerization by a solution polymerization method or the like, or bisphenol A
Epoxy resin such as epoxy resin, bisphenol F epoxy resin, cycloaliphatic epoxy resin, glycidyl ester epoxy resin, glycidylamine epoxy resin, hydantoin epoxy resin, triglycidyl isocyanurate, etc. , And combinations thereof.

In particular, it is preferable that the polyepoxy compound is an aqueous dispersion of an epoxy group-containing acrylic copolymer.
The production of the epoxy group-containing acrylic copolymer aqueous dispersion,
It can be carried out in the same manner as in the production of a carbonyl group-containing emulsion by selecting a monomer. The curable composition comprising the hydrazine derivative composition (A) of the present invention and the polycarbonyl compound (B) and / or the polyepoxy compound (C) has a solid content weight ratio of (A) / ((B ) +
(C)) = 0.1 / 99.9 to 90/10. As a result, a film having both low-temperature curability and storage stability and having excellent water resistance, stain resistance, hardness and the like can be provided. If the ratio is less than 0.1 / 99.9, the crosslinking density is low, and the effect of crosslinking is not exhibited, which is not preferable. If it exceeds 90/10, the resulting film becomes very brittle, which is not preferable.

The hydrazine derivative composition of the present invention can be mixed with a monoketone represented by the formula (2) for the purpose of controlling the reactivity with a polycarbonyl compound or a polyepoxy compound. R ⁴ R ⁵ C ＝ O (2) (wherein R ⁴ and R ⁵ are each a hydrogen atom, a linear or branched aliphatic residue having 2 to 20 carbon atoms,
It represents at least one selected from an alicyclic residue having 20 carbon atoms and an aromatic residue which may or may not have a substituent. R ⁴ and R ⁵ may form a cyclic structure. As the monoketones represented by the formula (2), 30 to
Those having a relatively low boiling point of 200 ° C. (for example, acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, etc.) are preferred because the reactivity can be easily controlled.

The hydrazine derivative composition of the present invention may contain a known carbonyl group-free ultraviolet absorber such as benzophenone, benzotriazole or triazine, or a known hindered phenol or hindered amine. A light stabilizer having no carbonyl group may be used in combination. The fourth curable composition of the present invention may contain, if necessary, components usually added to paints and the like, such as pigments, fillers, dispersants, wetting agents, thickeners, rheology control agents, defoamers, plasticizers An agent, a film-forming aid, a rust inhibitor, a dye, a preservative, and the like can be selected and combined in accordance with the respective purposes.

Further, the fourth curable composition of the present invention comprises a paint, a base material or a finishing material for building materials, an adhesive, an adhesive,
It is useful as a paper processing agent or a finishing material for woven or nonwoven fabrics. Examples of the paint, a base treatment material or a finishing material for a building material include inorganic building materials such as concrete, cement mortar, slate plate, scallop plate, gypsum board, extruded plate, foamable concrete, and building materials based on woven or nonwoven fabric. , Paint or architectural finishing materials for various bases such as metal building materials, furthermore, main materials and top coats for multi-layer finishing coating materials, thin finishing coating materials, thick finishing coating materials, stone finish finishing materials, gloss paint, etc. Examples include synthetic resin emulsion paints, paints for metals, wood paints, paints for tiles, and the like.
As the adhesive, for example, adhesives for automobile interiors, adhesives for building members, laminating adhesives for various films, etc., metals, plastics, wood, slate, paper,
Examples include a wet adhesive and a contact adhesive for cloth and the like. Examples of the pressure-sensitive adhesive include a permanent pressure-sensitive adhesive, a removable pressure-sensitive adhesive, and the like used for a single-sided tape, a double-sided tape, a label, an album, and the like.

[0084]

DESCRIPTION OF THE PREFERRED EMBODIMENTS Parts in the examples mean parts by weight. In addition, regarding the physical property test of the curable compositions obtained in Examples and Comparative Examples, a coating material was prepared using the curable composition with the following composition, and a test was performed according to the test method described below. . <Coating composition> Preparation of enamel coating composition Pigment dispersion Water 82.5 parts Dispersant: Poise 530 (product name, manufactured by Kao Corporation) 7.5 parts 5% aqueous solution of sodium tripolyphosphate 7.5 parts Viscosity: 3% aqueous solution of Daicel HEC SP-600 (product name, manufactured by Daicel Chemical Industries, Ltd.) 25.0 parts Antifoaming agent: Nopco 1497VD (product name, manufactured by San Nopco Co., Ltd.) 2.5 parts Rutile type Titanium oxide: Taipure R-900 (trade name, manufactured by DuPont) 375.0 parts Let-down component Curable compositions of the respective examples and comparative examples (solid content conversion) 460.0 parts Ethylene glycol monobutyl ether 45. 0 parts Water 30.0 parts Antifoaming agent: Nopco 1497VD (product name, manufactured by San Nopco Co., Ltd.) 1.0 part <Test method> Water resistance Yar coater No. 5
0, and applied to a sulfated alumite plate at room temperature (25
C) for 2 days. After further drying at 50 ° C. for 2 days, it was immersed in water at 40 ° C. for 30 days, and the state was visually determined. The criteria are as follows.

A: No blistering or shine is observed at all. ○: Some blisters are found, but no gloss is seen. Δ: Blisters and gloss are observed. ×: The entire surface is blistered and gloss is remarkable. Initial Gloss Value, Gloss Retention The above enamel paint formulation was prepared using a wire coater No. 5
0, and applied to a sulfated alumite plate at room temperature for 30 minutes.
Let dry for days. The 60 ° -60 ° specular reflectance at that time was measured as an initial gloss value (this is defined as the test start time of gloss retention, that is, zero time).

Subsequently, an exposure test (rain cycle: 12 minutes / hour, black panel temperature: 60 to 66 ° C.) was conducted using a sunshine type weatherometer (WEL-SUN-DC, manufactured by Suga Test Instruments Co., Ltd.). . The 60 ° -60 ° specular reflectance after 3000 hours of exposure was measured as the final gloss value, divided by the initial gloss value, and this value was calculated as the gloss retention. Molecular weight distribution Using gel permeation chromatography,
It was determined from a standard polystyrene calibration curve.

(Equipment used) · Apparatus: Tosoh Corporation HLC-8020 · Column: Tosoh Corporation TSKgel G-5000 HXL TSKgel G-4000 HXL TSKgel G-2000 HXL · Data processing: Tosoh Corporation SC8010 ・ Carrier: tetrahydrofuran

[0088]

Reference Example 1 Synthesis of polyhydrazine compound (1). 168 parts of hexamethylene diisocyanate and 1.5 parts of water as a buret agent were mixed with ethylene glycol methyl ether acetate and trimethyl phosphate at a ratio of 1: 1 (weight ratio).
Dissolved in 130 parts of a mixed solvent of
Allowed to react for hours. The resulting reaction solution was subjected to two-stage treatment under a condition of 1.0 mmHg / 160 ° C. in the first time using a thin-film distillation can under the condition of 1.0 mmHg / 160 ° C. And the solvent was removed by distillation.

The obtained polyisocyanate compound is a burette-type polyisocyanate of hexamethylene diisocyanate, having a residual hexamethylene diisocyanate of 0.1% by weight and a -NCO content of 23.3% by weight.
The viscosity is 1900 (± 200) mPa. s / 25 °, number average molecular weight is about 600 (± 100), average -NCO
The number of functional groups was about 3.3.

20 parts of hydrazine monohydrate was added at room temperature to 230 parts of isopropyl alcohol in a reactor having a reflux condenser, a thermometer and a stirrer. A solution prepared by dissolving 42 parts of the above burette-type polyisocyanate in 168 parts of tetrahydrofuran was added at 40 ° C. over about 1 hour, and stirring was continued at 40 ° C. for 3 hours.
The tetrahydrofuran, hydrazine, water and the like in the obtained reaction solution are distilled off under reduced pressure by heating to obtain a solid content of 30%.
% Aqueous solution of polyhydrazine compound (1)

[0091]

Reference Example 2 Synthesis of polyhydrazine compound (2). 1. 222 parts of isophorone diisocyanate, 168 parts of hexamethylene diisocyanate, water as a buret agent
4 parts of a 1: 1 (weight ratio) mixed solvent of ethylene glycol methyl ether acetate and trimethyl phosphate 13
0 parts, and reacted at a reaction temperature of 160 ° C. for 1.5 hours. The obtained reaction solution was first used under a condition of 1.0 mmHg / 160 ° C. and a
Excess isophorone diisocyanate and hexamethylene diisocyanate and the solvent were distilled off and recovered by a two-stage treatment under the condition of mHg / 200 ° C.

The obtained polyisocyanate compound is a coburet-type polyisocyanate of isophorone diisocyanate and hexamethylene diisocyanate. The remaining isophorone diisocyanate is 0.7% by weight, the remaining hexamethylene diisocyanate is 0.1% by weight, and -NCO
The content is 19.6% by weight and the viscosity is 20,000 (± 300
0) mPa · s / 40 ° C., number average molecular weight is about 800 (±
100) and the average -NCO functionality was about 3.7.

In a reactor equipped with a reflux condenser, a thermometer and a stirrer, 23 parts of acetone, 17.3 parts of the above-mentioned burette type polyisocyanate, and polyoxyethylene methyl ether (manufactured by NOF Corporation, product name: UNIOX M1)
000, a hydroxyl value of 56.9) and 10 parts of dibutyltin dilaurate as a catalyst were reacted at 60 ° C. for 4 hours. Next, 74 parts of hydrazine monohydrate was added to 421 parts of acetone placed in a reactor having a reflux condenser, a thermometer and a stirrer at room temperature over 30 minutes while stirring, and the mixture was further stirred for 1 hour. The reaction product obtained above was added to this reaction solution with stirring at 40 ° C. over 1 hour, and then further stirred at 40 ° C. for 4 hours. Then 1183
Of water at 40 ° C. over 30 minutes and stirring was continued for another 30 minutes. Acetone and ethyl acetate in the obtained reaction solution,
Hydrazine, a reaction product of acetone and hydrazine, water, and the like were distilled off under reduced pressure under heating to obtain an aqueous solution of a polyhydrazine compound (2) having a solid content of 30%.

[0094]

Reference Example 3 Synthesis of polyhydrazine compound (3). 8.9 parts of hydrazine monohydrate was added at room temperature to 103 parts of isopropyl alcohol in a reactor having a reflux condenser, a thermometer and a stirrer. The isocyanurate-type polyisocyanate of isophorone diisocyanate [product name: VESTANAT manufactured by Huls Japan K.K.
(Trademark) T-1890, number average molecular weight is about 800, average number of NCO groups is about 3.2, NCO group content is 16.4 wt.
%, 100% pellet product] A solution prepared by dissolving 23 parts of 92 parts of tetrahydrofuran was added at 10 ° C over about 1 hour, and stirring was continued at 40 ° C for 3 hours. afterwards,
While stirring the reaction system at 40 ° C., butyl cellosolve 50
Parts were added. The tetrahydrofuran, hydrazine, isopropyl alcohol, butyl cellosolve, and the like in the obtained reaction solution are distilled off under reduced pressure by heating to obtain a solid content of 50%.
% Of a butyl cellosolve solution of the polyhydrazine compound (2). 50 of the obtained polyhydrazine compound (3)
To 95 parts of a 95% butyl cellosolve solution, 2.7 parts of levulinic acid, 3.5 parts of a 10% aqueous ammonia solution, and 57 parts of water were added, followed by stirring at 30 ° C. for 1 hour to obtain a uniform transparent aqueous solution.

[0095]

Reference Example 4 Synthesis of polyhydrazine compound (4). A four-necked flask equipped with a stirrer, a thermometer, a reflux condenser, a nitrogen blowing tube, and a dropping funnel was set to a nitrogen atmosphere, and 600 parts of hexamethylene diisocyanate and a polyester polyol as a trihydric alcohol (Daicel Chemical Co., Ltd.
(Product name: Placcel 303), 30 parts of the reactor were kept at 90 ° C. for 1 hour under stirring to carry out a urethanization reaction. Thereafter, the temperature in the reactor was maintained at 60 ° C., tetramethylammonium capryate, an isocyanuration catalyst, was added, and when the yield became 54%, phosphoric acid was added to stop the reaction. After filtering the reaction solution, unreacted HMDI was removed using a thin film distillation still. The isocyanate content of the obtained polyisocyanate compound was 18.2%, the number average molecular weight was 1,100, and the average number of functional groups was 5.1.

A four-necked flask equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen blowing pipe was set to a nitrogen atmosphere.
200 parts of the above polyisocyanate compound, hydroxyl value 5
6.9 polyoxyethylene monomethyl ether (manufactured by NOF Corporation, product name: UNIOX M1000) 87
Parts, 460 parts of 1,4-dioxane, and 0.04 part of dibutyltin dilaurate as a catalyst, and the temperature in the reactor was maintained at 75 ° C. for 2 hours with stirring to add polyoxyethylene monomethyl ether to polyisocyanate. .

Next, the inside of the four-necked flask equipped with a stirrer, a thermometer, a reflux condenser, a nitrogen blowing pipe and a dropping funnel was set to a nitrogen atmosphere, and 404 parts of 2-butoxyethanol and 114 parts of hydrazine monohydrate were added. The mixture was stirred at 25 ° C for 30 minutes. The whole amount of the reaction solution of the polyisocyanate compound and polyoxyethylene monomethyl ether was added to this solution over 1 hour while stirring at 25 ° C., and further stirred at 25 ° C. for 1 hour.

1,4-dioxane in the obtained reaction solution,
2-Butoxyethanol, hydrazine monohydrate, water and the like were distilled off under heating and reduced pressure to obtain a 2-butoxyethanol solution of polyhydrazine compound (4) having a solid content of 80%.

[0099]

Reference Example 5 Preparation of polycarbonyl compound. In a reactor having a reflux condenser, a dropping tank, a thermometer and a stirring device,
218 parts of ion-exchanged water, surfactant (trade name: Adecaria Soap SE-1025N, manufactured by Asahi Denka Kogyo KK)
3.7 parts of a 5% aqueous solution was charged, and the temperature in the reaction vessel was set to 80.
℃, then 9 parts of methacrylic acid, styrene 4.
5 parts, 234 parts of butyl acrylate, 13.5 parts of diacetone acrylamide, 189 parts of methyl methacrylate, 225 parts of ion-exchanged water, Adecaria soap SE-1025
A mixture of 14.4 parts of N, 10 parts of a 25% aqueous solution of polyoxyethylene nonylphenyl ether (trade name: Emulgen 950, manufactured by Kao Corporation), and 1 part of ammonium persulfate was dropped into the reaction vessel from the dropping tank for 3 hours. And flowed in. During the inflow, the temperature in the reaction vessel was kept at 80 ° C. After the completion of the inflow, the temperature in the reaction vessel was kept at 80 ° C. and maintained for 2 hours. Then, the mixture was cooled to room temperature, the pH was adjusted to 8 by adding a 25% aqueous ammonia solution, and the mixture was filtered through a 100-mesh wire gauze. I got

[0100]

Example 1 A surfactant (manufactured by Kao Corporation, product name: Latemul ASK, solid content 28%) was added to 100 parts of a 30% aqueous solution of the polyhydrazine compound (1) obtained in Reference Example 1.
6.7 parts and 8.4 parts of 2,2,6,6-tetramethyl-4-piperidone were added and mixed to obtain a hydrazine derivative composition (1).

[0101]

Example 2 To 40 parts of a 30% aqueous solution of the polyhydrazine compound (2) obtained in Reference Example 2, 29.5 parts of a 10% aqueous solution of 2,2,6,6-tetramethyl-4-piperidone was added. Hydrazine derivative composition (2) by mixing
I got

[0102]

Example 3 40 parts of an aqueous solution of the polyhydrazine compound (3) obtained in Reference Example 3 was added to N-methyl-2,2,6,6
By adding and mixing 1.4 parts of tetramethyl-4-piperidone, a hydrazine derivative composition (3) was obtained.

[0103]

Example 4 To 50 parts of an aqueous solution of the polyhydrazine compound (4) obtained in Reference Example 4 in 2-butoxyethanol was added.
After adding and mixing 5.8 parts of N-methyl-2,2,6,6-tetramethyl-4-piperidone, 77.5 parts of water is added and mixed to obtain a hydrazine derivative composition (4).
I got

[0104]

Example 5 9.3 parts of the hydrazine derivative composition (1) obtained in Example 1 was added to 100 parts of the carbonyl group-containing copolymer aqueous emulsion synthesized in Reference Example 5 and mixed to obtain a curable resin. A composition was obtained. A coating material was prepared using the obtained curable composition and subjected to each test. Table 1 shows the results.

[0105]

Example 6 1100 parts of the hydrazine derivative composition (4) obtained in Example 4 was added to 100 parts of the aqueous carbonyl group-containing copolymer aqueous emulsion synthesized in Reference Example 5 and mixed to obtain a curable resin. A composition was obtained. A coating material was prepared using the obtained curable composition and subjected to each test. Table 1 shows the results.

[0106]

Example 7 11.7 parts of the hydrazine derivative composition (2) obtained in Example 2 was added to 100 parts of the carbonyl group-containing copolymer aqueous emulsion synthesized in Reference Example 5 and mixed to obtain a curable resin. A composition was obtained. A coating material was prepared using the obtained curable composition and subjected to each test. Table 1 shows the results.

[0107]

Comparative Example 1 A coating material was prepared using only the aqueous emulsion containing a carbonyl group-containing copolymer synthesized in Reference Example 5 and used for each test. Table 1 shows the results.

[0108]

Comparative Example 2 To 100 parts of the aqueous carbonyl group-containing copolymer aqueous emulsion synthesized in Reference Example 5, 6.1 parts of a 30% aqueous solution of the polyhydrazine compound (1) obtained in Reference Example 1 was added and mixed. A curable composition was obtained. A coating material was prepared using the obtained curable composition and subjected to each test.
Table 1 shows the results.

[0109]

[Table 1]

[0110]

By using the hydrazine derivative composition of the present invention as a curing agent for a polycarbonyl compound or a polyepoxy compound, it is excellent in weather resistance, high in cross-linking density, tough, water-resistant, chemical-resistant and heat-resistant. A film excellent in properties and the like can be obtained.

──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. ⁷ Identification symbol FI Theme coat ゛ (Reference) // C09D 133/14 C09D 133/14 179/06 179/06 C09J 133/14 C09J 133/14 179/06 179/06

Claims (7)

[Claims] 1. A hydrazine derivative composition comprising a polyhydrazine compound having two or more hydrazine residues in one molecule, a light stabilizer having a carbonyl group and / or an ultraviolet absorber having a carbonyl group. 2. The hydrazine derivative composition according to claim 1, wherein the polyhydrazine compound is a semicarbazide derivative composition represented by the formula (1). Embedded image (Wherein R ¹ is a linear or branched C 2-20
Alkylene diisocyanate, cycloalkylene diisocyanate having 5 to 25 carbon atoms which may or may not have a substituent, arylene diisocyanate having 6 to 20 carbon atoms which may or may not have a substituent, and A terminal isocyanate group derived from a trimer to 20-mer oligomer of at least one diisocyanate selected from the group consisting of aralkylene diisocyanates having 8 to 20 carbon atoms which may or may not have a substituent; polyisocyanate residues without triisocyanate residue or R ¹ is derived from alkylene diisocyanates having 2 to 20 carbon atoms which is substituted with isocyanatoalkyl group having 1 to 8 carbon atoms, without the terminal isocyanate groups, Represents R ²
Each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms. R ³ is a linear or branched alkylene group having 1 to 20 carbon atoms, a cycloalkylene group having 5 to 20 carbon atoms, or a 6 to 10 carbon atoms which may or may not have a substituent. Represents an arylene group. n is 0 or 1
Represents l and m each represent 0 or a positive integer. However, 20 ≧ (l + m) ≧ 3. ) 3. The hydrazine derivative composition according to claim 1, wherein the light stabilizer having a carbonyl group is a hindered amine derivative. 4. A curable composition comprising the hydrazine derivative composition according to claim 1 and a polycarbonyl compound and / or a polyepoxy compound. 5. The curable composition according to claim 4, comprising a monoketone represented by the formula (2). R ⁴ R ⁵ C ＝ O (2) (wherein R ⁴ and R ⁵ are each a hydrogen atom, a linear or branched aliphatic residue having 2 to 20 carbon atoms,
Represents an alicyclic residue having 20 carbon atoms, or an aromatic residue which may or may not have a substituent. R ⁴ , R ⁵
May form a ring structure. ) 6. The polycarbonyl compound is a carbonyl group-containing acrylic copolymer aqueous dispersion.
The curable composition according to the above. 7. The curable composition according to claim 4, wherein the polyepoxy compound is an aqueous dispersion of an acrylic copolymer containing an epoxy group.